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Operational and safety protocols for neurologic monoclonal antibodies (mAbs) must be precisely matched to disease biology and operational strategy, including mandatory B‑cell and infection monitoring in multiple sclerosi...

Join ICON Biotech at OCT East Coast 2026, taking place 12–13 May 2026 at the Hyatt Regency New Brunswick, New Jersey. Meet our team at Booth \#25 and explore how our specialised clinical development services can suppor...

Are you working with NONMEM or PDx-Pop? Don’t miss the chance to connect with our team at PAGE in Croatia. Visit us at booth \#2 to: - Explore the latest features in NONMEM and PDx-Pop - Get expert insights on populati...

Heading to Philadelphia for #ISPORAnnual? Our ICON HEOR and RWE teams will be on-site sharing the latest thinking on patient-centred outcomes, comparative effectiveness research, and innovative evidence synthesis. Let’...

If recruitment and retention matter, site satisfaction must be treated as a prerequisite. In this Journal for Clinical Studies article, Brian Mallon explains why start-up success is shaped by human factors, not technolog...

We’re proud to share that Rose Kidd, President of Operational Delivery at ICON, has been recognised at the Women in Pharma Awards 2026, winning Excellence in senior leadership – life sciences. This award reflects Rose’...

May is Mental Health Awareness Month. More than one in five adults in the US experience mental illness and the average delay between onset of symptoms and treatment is 11 years. Explore ICON’s experience in over 100 ps...

Ankita Minhas will speak on 6 May at OCT Europe in Barcelona at 12:00pm in Stream C. Her session will explore how leading biotechs manage rising complexity through AI-driven innovation, smarter trial designs, and stronge...

Meet the ICON team at SCDM #EMEA26, to discover how we are driving innovation in clinical data science and helping organisations build smarter, more resilient clinical programmes. Visit us at booth 11 to explore how IC...

What is it really like to build a career as a Senior Clinical Research Associate at ICON? In our latest careers blog, Rafi Cabral, MD ,CCRP shares his experience of life as a CRA, from partnering with study sites and su...

Do you struggle to keep on top of regulatory changes affecting the world of medicine and medical device clinical trials? Join thousands of subscribers who have discovered the convenience of our free monthly publication b...

Participant-centric study design has advanced, but site-centric execution has not kept pace. In the Journal for Clinical Studies, Brian Mallon examines how unclear expectations, administrative burden and contract delays ...